Fractional Business Development Partner (independent contractor, commission-first) — U.S. BioPharma & MedTech consulting services jobs in United States
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Lumis International GmbH · 1 day ago

Fractional Business Development Partner (independent contractor, commission-first) — U.S. BioPharma & MedTech consulting services

LUMIS International represents U.S. BioPharma and MedTech companies in Europe, providing regulatory consulting and legal representation. The role involves cross-selling regulatory consulting services to existing clients and expanding the client base through new referrals and partnerships.

BiotechnologyConsultingOutsourcingTherapeutics

Responsibilities

Work a named list of existing Legal Representative clients (we’ll provide contacts)
Map the right people (regulatory, clinical operations, program leads) and secure intro calls
Run short discovery, identify near-term regulatory needs (e.g., ODD, submissions), and coordinate quotes with our consultants
Keep notes and next steps in the CRM; send a brief weekly summary (meetings booked, proposals out, deals moving)
Move opportunities to a signed project agreement and hand over cleanly to delivery
Set up referral/coop relationships with CROs and other partners
Prospect look-alike sponsors (same size/therapeutic focus) and book first meetings
Maintain a steady pipeline: new meetings, proposals, and signed projects each month
1-2 quality meetings a week from the named list in Phase 1
Scoping of deals to support our Proposals department
Every active deal has a next step and date in the CRM list

Qualification

BioPharma sales experienceMedTech sales experienceRegulatory consultingCRM proficiencyIndependent contractorCommunication skillsRelationship building

Required

5+ years selling services to BioPharma or MedTech sponsors (e.g., clinical trial services, CDMO, regulatory/quality/safety consulting, or clinical tech sold to sponsors)
Existing contacts in regulatory and/or clinical functions in the U.S
Track record closing service projects in the $25k–$250k+ range
Comfortable working as an independent contractor on a commission-first basis; reliable communication and consistent CRM use

Preferred

Rare disease and ODD experience; familiarity with EU regulators; prior U.S.–EU study work
Existing relationships with CROs or specialist consultancies

Benefits

Optional bonus per qualified meeting

Company

Lumis International GmbH

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Lumis International GmbH - Your partner in clinical efficacy For Drug development companies not located in the European Union Lumis offers to act as their legal representative according to the EU Clinical Trial Directive 2001/20/EC Art.

Funding

Current Stage
Early Stage

Leadership Team

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Heike Schoen
Co-Founder & Managing Director
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